Variant · Snv
RHBDF2 NM_001005498.4(RHBDF2):c.1029C>T (p.Gly343=)
CI-VAR-00053119Explore in graph →p.Gly343=NM_001005498.4:c.1029C>TClinVar 325443 rs61742551
Curated evidence
Evidence by cancer (0 items)
Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.
Data not yet available
No curated evidence item references this variant yet.
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
clinvarProvenance
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 325443 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Palmoplantar keratoderma-esophageal carcinoma syndrome; RHBDF2-related disorder; Malignant lymphoma, large B-cell, diffuse; Colorectal cancer; Cholangiocarcinoma; Malignant tumor of esophagus; Sarcoma; Ovarian serous cystadenocarcinoma; Uterine carcinosarcoma; Colon adenocarcinoma; Thymoma; Acute myeloid leukemia; Nonpapillary renal cell carcinoma | germline | 6 | Jan 27, 2026 | clinvar |